Responsibilities may include the following and other duties may be assigned. Directs or performs coordination and preparation of document packages for EU MDR regulatory submissions from all areas of company. Leads or compiles all materials required in submissions. Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.

1st exam they kept an assessment to check the standards of the students and then an interview. the interview was difficult and about the laws and in details about the indian laws, also about the basic C language, aptitude